Canonical Allele Identifier: CA937672232

Gene: NDUFS3

Linked Data

• dbSNP Id: rs2097269149
• gnomAD v3: 11-47582277-G-A
• gnomAD v4: 11-47582277-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582277G>A , CM000673.2:g.47582277G>A	GRCh38
NC_000011.9:g.47603829G>A , CM000673.1:g.47603829G>A	GRCh37
NC_000011.8:g.47560405G>A	NCBI36
NG_011946.1:g.8268G>A
NG_011946.2:g.8268G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.507+64G>A MANE Select	ENSP00000263774.4:n.507+64G>A
ENST00000531351.2:n.1631G>A
ENST00000677462.1:n.2981+64G>A
ENST00000678975.1:n.2764+64G>A
ENST00000263774.8:c.507+64G>A	ENSP00000263774.4:n.507+64G>A
ENST00000524568.1:n.610+64G>A
ENST00000525212.1:n.162+64G>A
ENST00000525378.5:n.445+64G>A
ENST00000527178.1:n.36G>A
ENST00000533507.5:n.1401+64G>A
NM_004551.2:c.507+64G>A	NP_004542.1:n.507+64G>A
NM_004551.3:c.507+64G>A MANE Select	NP_004542.1:n.507+64G>A